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Comparison of NOSE and Conventional Methods in Laparoscopic Right Colon Surgery

Primary Purpose

Surgical Incision

Status
Completed
Phase
Not Applicable
Locations
Turkey
Study Type
Interventional
Intervention
natural orifice
Sponsored by
Inonu University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional health services research trial for Surgical Incision

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • laparoscopic right hemicolectomy patients

Exclusion Criteria:

  • no

Sites / Locations

  • Inonu University

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

natural orifice

conventional

Arm Description

Patients who underwent laparoscopic surgery and removed the specimen from the natural orifice will be gathered. demographic data and perioperative results will be compiled

patients who underwent laparoscopic surgery and removed specimen with conventional will be gathered. demographic data and perioperative results will be compiled. (conventional extraction is suprapubic or median incision)

Outcomes

Primary Outcome Measures

VAS control
Visual Analog Score for pain (1-10 score)

Secondary Outcome Measures

Full Information

First Posted
February 3, 2018
Last Updated
October 10, 2019
Sponsor
Inonu University
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1. Study Identification

Unique Protocol Identification Number
NCT03487289
Brief Title
Comparison of NOSE and Conventional Methods in Laparoscopic Right Colon Surgery
Official Title
Comparison of NOSE and Conventional Methods in Laparoscopic Right Colon Surgery
Study Type
Interventional

2. Study Status

Record Verification Date
October 2019
Overall Recruitment Status
Completed
Study Start Date
January 1, 2013 (Actual)
Primary Completion Date
March 25, 2019 (Actual)
Study Completion Date
March 28, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Inonu University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
Laparoscopic right hemicolectomy (LRH) is an accepted surgical procedure for several right sided colonic pathologies. Recently the advantages of the intracorporeal ileotransversostomy over the extracorporeal anastomosis is appearing in the literature. Additionally, specimen extraction through the natural orifices is an emerging method when combined with the totally laparoscopic procedures. Our observations on natural orifice surgery was promising . In our daily surgical practice, investigators prefer the intracorporeal anastomosis and this study was conducted to compare the specimen extraction sites after LRH. Here investigators aimed to compare the results of conventional and natural orifice specimen extractions (NOSE) after totally LRHs.
Detailed Description
compare the patient-selected NOSE method and conventional method in laparoscopic right colon cancer surgery

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Surgical Incision

7. Study Design

Primary Purpose
Health Services Research
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Non-Randomized
Enrollment
52 (Actual)

8. Arms, Groups, and Interventions

Arm Title
natural orifice
Arm Type
Experimental
Arm Description
Patients who underwent laparoscopic surgery and removed the specimen from the natural orifice will be gathered. demographic data and perioperative results will be compiled
Arm Title
conventional
Arm Type
No Intervention
Arm Description
patients who underwent laparoscopic surgery and removed specimen with conventional will be gathered. demographic data and perioperative results will be compiled. (conventional extraction is suprapubic or median incision)
Intervention Type
Procedure
Intervention Name(s)
natural orifice
Other Intervention Name(s)
conventional
Intervention Description
laparoscopic right colon surgery and patients who are removed from the natural orifice and conventional will gather
Primary Outcome Measure Information:
Title
VAS control
Description
Visual Analog Score for pain (1-10 score)
Time Frame
6 years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: laparoscopic right hemicolectomy patients Exclusion Criteria: no
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ersin Gündoğan
Organizational Affiliation
Inonu Unıversity- general surgery
Official's Role
Principal Investigator
Facility Information:
Facility Name
Inonu University
City
Malatya
ZIP/Postal Code
44090
Country
Turkey

12. IPD Sharing Statement

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Comparison of NOSE and Conventional Methods in Laparoscopic Right Colon Surgery

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